Miller syndrome 66038001
SNOMED CT code
SNOMED code | 66038001 |
---|---|
name | Miller syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Miller syndrome (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Limb structure 66019005 |
Associated morphology | Morphologically abnormal structure 49755003 |
attributes - group3 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Bone structure 272673000 |
Associated morphology | Dysplasia 25723000 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Disorder of skeletal system 88230002 Skeletal dysplasia 105986008 Miller syndrome 66038001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Multiple malformation syndrome with facial-limb defects as major feature 23359005 Miller syndrome 66038001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Miller syndrome 66038001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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